GHRLOS

Chr 3

ghrelin opposite strand/antisense RNA

Also known as: GHRL-AS1, GHRLAS, NCRNA00068

This antisense gene regulates the ghrelin/obestatin prepropeptide gene through non-coding regulatory RNAs produced by alternative splicing. Mutations cause autosomal dominant Silver-Russell syndrome, a growth disorder characterized by severe intrauterine and postnatal growth restriction, relative macrocephaly, and distinctive facial features with onset in infancy. The gene shows high constraint against loss-of-function variants, indicating its critical regulatory role in growth and development.

OMIMResearchSummary from RefSeq

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

0 submitted variants in ClinVar

Protein Context — Lollipop Plot

GHRLOS · protein map & ClinVar variants

Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.

3D Protein StructureAlphaFold

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →
Clinical Literature
Open Research Assistant →